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- Klinische proef NCT02176499
Natriuretic Effect of Telmisartan Versus Placebo in Patients With Mild-to-Moderate Hypertension
7 juli 2014 bijgewerkt door: Boehringer Ingelheim
Natriuretic Effect of Telmisartan Versus Placebo in Patients With Mild-to-Moderate Hypertension On a Controlled Sodium Diet (100 mmol/Day)
Study to compare the natriuretic effect of telmisartan to placebo in mild-to-moderate hypertensive patients on a controlled sodium diet as well as to explore the effects of telmisartan on norepinephrine, plasma renin activity (PRA), plasma aldosterone, urine potassium, creatinin, chloride, bicarbonate and uric acid excretion.
Additionally it was assessed whether the natriuretic effect disappears after treatment when telmisartan is stopped.
The effects of telmisartan on seated clinic blood pressure and the relationship between urine sodium loss and decrease in ambulatory blood pressure after the first dose were assessed descriptively.
Assessment of safety was also considered.
Studie Overzicht
Toestand
Voltooid
Conditie
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Werkelijk)
26
Fase
- Fase 3
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
18 jaar tot 65 jaar (Volwassen, Oudere volwassene)
Accepteert gezonde vrijwilligers
Nee
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
Inclusion Criteria:
- Mild-to-moderate hypertension as defined by a morning mean diastolic blood pressure from ≥ 90 and ≤ 115 mmHg and a mean systolic blood pressure ≤ 200 mmHg after five minutes in the seated position at the end of three weeks of placebo run-in treatment
- Male or female patients between 18 and 65 years of age, inclusive. Patients 60 to 65 years of age must have a screening 24-hour urine creatinine clearance rate of ≥ 1 mL/sec
- Ability to provide written informed consent
Exclusion Criteria:
- Pre-menopausal women (last menstruation ≤ one year to start of screening)
Post-menopausal women (last menstruation > one year from start of screening or have had a hysterectomy and oophorectomy)
- Who have < three months of stable estrogen replacement therapy at screening
- Who will be on progesterone therapy at any time during the trial
- Known or suspected secondary hypertension
Hepatic and/or renal dysfunction as defined by the following laboratory parameters:
- ALT (alanine aminotransferase) or AST (aspartate aminotransferase) greater than two times the upper limit of reference range
- Serum creatinine greater than 2.3 mg/dL
- Bilateral renal artery stenosis; renal artery stenosis in a solitary kidney; post-renal transplant
- NYHA (New York Heart Association) functional class CHF (chronic heart failure) III-IV
- Unstable angina, myocardial infarction or cardiac surgery within the preceding three months
- Stroke within the preceding six months
- PTCA (percutaneous transluminal coronary angioplasty) within the preceding three months
- History of angioedema
- Sustained ventricular tachycardia, atrial fibrillation, or other clinically relevant cardiac arrhythmias as determined by the clinical Investigator
- Hypertrophic obstructive cardiomyopathy, aortic stenosis, hemodynamically relevant stenosis of aortic or mitral valve
- Administration of digoxin or other digitalis-type drugs
- Patients with insulin-dependent and non-insulin-dependent diabetes mellitus
- History of drug or alcohol dependency
- Use of antihypertensive agents such as diuretics, ACE inhibitors, angiotensin II antagonists, α-blockers, β-blockers, calcium channel antagonists, direct vasodilators at any time during the trial
- Administration of other non-antihypertensive medications known to affect blood pressure (e.g., oral corticosteroids, MAO (monoamine oxidase) inhibitors, nitrates) at any time during the trial
- Chronic administration of high doses of NSAIDS and aspirin (e.g., ibuprofen for rheumatoid arthritis and osteoarthritis in total daily dose in excess of 1600 mg, aspirin in excess of 2 Gm per day)
- Chronic use of salt substitutes containing potassium chloride; potassium supplements; extreme dietary restrictions
- Clinically significant sodium depletion as defined by a serum sodium level less than 130 mEq/L
- Clinically significant hyperkalemia as defined by a serum potassium level greater than 6.0 mEq/L. Clinically significant hypokalemia as defined by a serum potassium level less than 3.0 mEq/L
- Patients receiving any investigational therapy within one month of signing the informed consent form. Note that patients who have participated in previous telmisartan studies may participate in this study provided there has been at least one month between discontinuing the previous study and signing the consent for the present study
- Known hypersensitivity to any component of telmisartan
- Any other clinical condition which, in the opinion of the principal Investigator, would not allow safe completion of the protocol and safe administration of trial medication
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Dubbele
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: Telmisartan, low dose
3 weeks placebo run-in (normal diet), 1 week placebo run-in (controlled sodium diet), 2 weeks double-blind treatment ,1 week placebo wash-out (controlled sodium diet)
|
|
|
Experimenteel: Telmisartan, high dose
3 weeks placebo run-in (normal diet), 1 week placebo run-in (controlled sodium diet), 2 weeks double-blind treatment, 1 week placebo wash-out (controlled sodium diet)
|
|
|
Placebo-vergelijker: Placebo
3 weeks placebo run-in (normal diet), 1 week placebo run-in (controlled sodium diet), 2 weeks double-blind treatment, 1 week placebo wash-out (controlled sodium diet)
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Cumulative urinary sodium loss
Tijdsspanne: 0-4, 4-8, 8-24 hours post-dose at baseline, day 0, day 7 and 0-24 hours post-dose on days 1-6
|
0-4, 4-8, 8-24 hours post-dose at baseline, day 0, day 7 and 0-24 hours post-dose on days 1-6
|
Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Cumulative urine sodium loss
Tijdsspanne: 0-24 hours post-dose on days 8-13 and 0-4, 4-8, 8-24 hours post-dose on day 14
|
0-24 hours post-dose on days 8-13 and 0-4, 4-8, 8-24 hours post-dose on day 14
|
|
Changes in body weight
Tijdsspanne: 24 hours post-dose on days -28, -21 to -14, -7, -1, 0, 7, 14 and 22
|
24 hours post-dose on days -28, -21 to -14, -7, -1, 0, 7, 14 and 22
|
|
Changes in plasma norepinephrine
Tijdsspanne: Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
|
Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
|
|
Changes in renin activity
Tijdsspanne: Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
|
Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
|
|
Changes in aldosterone
Tijdsspanne: Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
|
Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
|
|
Changes in urine potassium
Tijdsspanne: Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
|
Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
|
|
Changes in creatinine chloride
Tijdsspanne: Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
|
Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
|
|
Changes in bicarbonate
Tijdsspanne: Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
|
Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
|
|
Changes in uric acid
Tijdsspanne: Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
|
Baseline, on day 0 after the end of the 24 hour dosing interval, on days 7, 14 and 22
|
|
Cumulative urinary sodium gain during wash-out period
Tijdsspanne: 0-24 hours post-dose on days from day 15 to 22
|
0-24 hours post-dose on days from day 15 to 22
|
|
Changes in seated clinic blood pressure
Tijdsspanne: Baseline and day 14
|
Baseline and day 14
|
|
Changes in 24 hour ambulatory Blood Pressure (ABPM) after the first dose of telmisartan
Tijdsspanne: Day 0
|
Day 0
|
|
Number of patients with adverse events
Tijdsspanne: up to 50 days
|
up to 50 days
|
|
Number of patients with abnormal findings in physical examination
Tijdsspanne: Baseline and day 22
|
Baseline and day 22
|
|
Number of patients with abnormal findings in 12-lead electrocardiogram (ECG)
Tijdsspanne: Baseline and day 22
|
Baseline and day 22
|
|
Number of patients with abnormal changes in laboratory parameters
Tijdsspanne: Baseline and day 22
|
Baseline and day 22
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Publicaties en nuttige links
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Nuttige links
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start
1 februari 1999
Primaire voltooiing (Werkelijk)
1 juli 1999
Studieregistratiedata
Eerst ingediend
26 juni 2014
Eerst ingediend dat voldeed aan de QC-criteria
26 juni 2014
Eerst geplaatst (Schatting)
27 juni 2014
Updates van studierecords
Laatste update geplaatst (Schatting)
8 juli 2014
Laatste update ingediend die voldeed aan QC-criteria
7 juli 2014
Laatst geverifieerd
1 juli 2014
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 502.255
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